LDH info

Canonical Allele Identifier: CA3741127
Gene: C6orf10 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2273017

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32369853G>A , CM000668.2:g.32369853G>A GRCh38
NC_000006.11:g.32337630G>A , CM000668.1:g.32337630G>A GRCh37
NC_000006.10:g.32445608G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001286474.1:c.100+44C>T VV NP_001273403.1:p.=
NM_001286475.1:c.100+44C>T VV NP_001273404.1:p.=
NM_006781.4:c.100+44C>T VV NP_006772.3:p.=
XM_011514235.1:c.100+44C>T XP_011512537.1:p.=
XM_011514236.1:c.100+44C>T XP_011512538.1:p.=
XM_011514237.1:c.100+44C>T XP_011512539.1:p.=
XM_011514238.1:c.100+44C>T XP_011512540.1:p.=
XM_011514239.1:c.100+44C>T XP_011512541.1:p.=
XM_011514240.1:c.100+44C>T XP_011512542.1:p.=
XM_011514241.1:c.100+44C>T XP_011512543.1:p.=
XM_011514242.1:c.100+44C>T XP_011512544.1:p.=
XM_011514243.1:c.100+44C>T XP_011512545.1:p.=
XM_011514244.1:c.100+44C>T XP_011512546.1:p.=
XM_011514245.1:c.100+44C>T XP_011512547.1:p.=
XM_011514246.1:c.100+44C>T XP_011512548.1:p.=
XM_011515039.1:c.481+4014G>A XP_011513341.1:p.=
XM_011515040.1:c.481+4014G>A XP_011513342.1:p.=
NR_136244.1:n.500+4014G>A
NR_136245.1:n.302+4014G>A
XM_024446307.1:c.100+44C>T XP_024302075.1:p.=
NM_001286474.2:c.100+44C>T VV NP_001273403.1:p.=
NM_001286475.2:c.100+44C>T VV NP_001273404.1:p.=
NM_006781.5:c.100+44C>T VV NP_006772.3:p.=
ENST00000375007.8:c.100+44C>T ENSP00000364146.4:p.=
ENST00000375015.8:c.100+44C>T ENSP00000364155.4:p.=
ENST00000442822.6:c.100+44C>T ENSP00000411164.2:p.=
ENST00000447241.6:c.100+44C>T ENSP00000415517.2:p.=
ENST00000527965.5:c.100+44C>T ENSP00000435103.1:p.=
ENST00000532023.5:c.100+44C>T ENSP00000432814.1:p.=
ENST00000533191.5:c.100+44C>T ENSP00000431199.1:p.=
ENST00000534588.1:c.100+44C>T ENSP00000432566.1:p.=
ENST00000612031.4:c.100+44C>T ENSP00000480403.1:p.=
ENST00000617061.4:c.100+44C>T ENSP00000482001.1:p.=